Department of Radiological Sciences, University of Rome La Sapienza, V.le Regina Elena 324, 00161 Rome, Italy.
Radiology. 2010 Dec;257(3):653-61. doi: 10.1148/radiol.10100732. Epub 2010 Sep 30.
To prospectively determine the diagnostic performance of breast magnetic resonance (MR) imaging in predicting the malignancy of breast lesions classified as borderline at core needle biopsy (CNB).
This prospective study was approved by the local ethics committee, and all patients provided written informed consent. Between February 2007 and October 2009, 193 patients underwent ultrasonography (US)-guided CNB. Thirty-two lesions in 32 patients were classified as "borderline" ("lesions of uncertain malignant potential" according to the United Kingdom National Health Service Breast Screening program or those that are "probably benign" according to the Breast Imaging Reporting and Data System [BI-RADS] lexicon) at pathologic examination and were evaluated. All 32 patients underwent contrast agent-enhanced breast MR imaging 1-3 weeks after CNB; surgical biopsy was performed within 60 days of MR imaging. Results were compared with histologic findings. Sensitivity, specificity, accuracy, and positive and negative predictive values were calculated.
Findings from surgical biopsy confirmed the diagnosis of seven atypical ductal hyperplasia lesions, four atypical lobular hyperplasia (ALH) lesions, five papillary lesions, two fibroepithelial lesions, three radial scars, three lobular carcinomas in situ, three ductal carcinomas in situ (DCIS), four invasive ductal carcinomas, and one invasive lobular carcinoma. With regard to malignancy, breast MR imaging helped correctly classify 22 of the 32 lesions as negative and seven as positive. Two of the lesions confirmed to be ALH were incorrectly classified as suspicious (BI-RADS category IV; false-positive finding), whereas one small DCIS was incorrectly classified as nonsuspicious (BI-RADS category II; false-negative finding). The sensitivity, specificity, accuracy, and positive and negative predictive values for the correct demonstration of malignancy at MR imaging were 88% (seven of eight lesions), 92% (22 of 24 lesions), 91% (29 of 32 lesions), 78% (seven of nine lesions), and 96% (22 of 23 lesions), respectively.
Breast MR imaging can improve the evaluation of lesions classified as borderline at CNB. In cases of nonsuspicious enhancement or no enhancement at breast MR imaging, follow-up rather than surgical biopsy might be performed.
前瞻性地确定乳腺磁共振(MR)成像在预测经核心针活检(CNB)诊断为边界病变的乳腺癌的诊断性能。
本前瞻性研究经当地伦理委员会批准,所有患者均签署书面知情同意书。2007 年 2 月至 2009 年 10 月期间,193 例患者接受了超声(US)引导下的 CNB。32 例患者的 32 个病灶在病理检查中被归类为“边界”(根据英国国民健康服务乳腺筛查计划为“不确定恶性潜能的病变”或根据乳腺成像报告和数据系统[BI-RADS]词汇为“可能良性”),并进行了评估。所有 32 例患者在 CNB 后 1-3 周行对比增强乳腺 MR 成像检查;MR 成像后 60 天内行手术活检。结果与组织学发现进行比较。计算了敏感性、特异性、准确性、阳性和阴性预测值。
手术活检结果证实 7 例为不典型导管增生病变,4 例为不典型小叶增生(ALH)病变,5 例为乳头状病变,2 例纤维上皮病变,3 例放射状瘢痕,3 例小叶原位癌,3 例导管原位癌(DCIS),4 例浸润性导管癌和 1 例浸润性小叶癌。关于恶性肿瘤,乳腺 MR 成像正确分类了 32 个病灶中的 22 个为阴性,7 个为阳性。2 例证实为 ALH 的病变被错误地归类为可疑(BI-RADS 类别 IV;假阳性发现),而 1 例小的 DCIS 被错误地归类为非可疑(BI-RADS 类别 II;假阴性发现)。MR 成像正确显示恶性肿瘤的敏感性、特异性、准确性、阳性和阴性预测值分别为 88%(8 个病灶中的 7 个)、92%(24 个病灶中的 22 个)、91%(32 个病灶中的 29 个)、78%(9 个病灶中的 7 个)和 96%(23 个病灶中的 22 个)。
乳腺 MR 成像可改善对 CNB 诊断为边界病变的评估。在 MR 成像显示非可疑强化或无强化的情况下,可以进行随访而非手术活检。